Evidence map›Paper›PMID 39578525›Full record

ArticleScientific reports2024

A novel deep learning approach to identify embryo morphokinetics in multiple time lapse systems.

Guillaume Canat, Antonin Duval, Nina Gidel-Dissler, Alexandra Boussommier-Calleja

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Guillaume Canat *ImVitro, AI Team, Paris, France.
Antonin Duval *ImVitro, AI Team, Paris, France.
Nina Gidel-DisslerImVitro, AI Team, Paris, France.
Alexandra Boussommier-CallejaImVitro, AI Team, Paris, France. alexandra@im-vitro.com.

Funding

Bpifrance DOS0152872/00
6 · The paper itself

Abstract

The use of time lapse systems (TLS) in In Vitro Fertilization (IVF) labs to record developing embryos has paved the way for deep-learning based computer vision algorithms to assist embryologists in their morphokinetic evaluation. Today, most of the literature has characterized algorithms that predict pregnancy, ploidy or blastocyst quality, leaving to the side the task of identifying key morphokinetic events. Using a dataset of N = 1909 embryos collected from multiple clinics equipped with EMBRYOSCOPE/EMBRYOSCOPE+ (Vitrolife), GERI (Genea Biomedx) or MIRI (Esco Medical), this study proposes a novel deep-learning architecture to automatically detect 11 kinetic events (from 1-cell to blastocyst). First, a Transformer based video backbone was trained with a custom metric inspired by reverse cross-entropy which enables the model to learn the ordinal structure of the events. Second, embeddings were extracted from the backbone and passed into a Gated Recurrent Unit (GRU) sequence model to account for kinetic dependencies. A weighted average of 66.0%, 67.6% and 66.3% in timing precision, recall and F1-score respectively was reached on a test set of 278 embryos, with a model applicable to multiple TLS.

Indexed as

BlastocystDeep LearningEmbryonic DevelopmentFertilization in VitroTime-Lapse ImagingAlgorithmsEmbryo Culture TechniquesEmbryo, MammalianFemaleHumansKineticsPregnancyEmbryologyMachine learningMedical Imaging

Identifiers

PMID39578525
PMCPMC11584792

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.